dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs1487293579
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr14:88574787 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- A>C / A>G
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
None
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- ZC3H14 : Missense Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
Help
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
None
Help
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Genomic Placements
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 14 | NC_000014.9:g.88574787A>C |
| GRCh38.p14 chr 14 | NC_000014.9:g.88574787A>G |
| GRCh37.p13 chr 14 | NC_000014.8:g.89041131A>C |
| GRCh37.p13 chr 14 | NC_000014.8:g.89041131A>G |
| ZC3H14 RefSeqGene | NG_050601.1:g.16879A>C |
| ZC3H14 RefSeqGene | NG_050601.1:g.16879A>G |
Gene: ZC3H14, zinc finger CCCH-type containing 14
(plus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| ZC3H14 transcript variant 4 | NM_207662.4:c. | N/A | Genic Upstream Transcript Variant |
| ZC3H14 transcript variant 1 | NM_024824.5:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 1 | NP_079100.2:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 1 | NM_024824.5:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 1 | NP_079100.2:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 20 | NM_001326308.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 20 | NP_001313237.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 20 | NM_001326308.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 20 | NP_001313237.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 21 | NM_001326309.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 21 | NP_001313238.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 21 | NM_001326309.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 21 | NP_001313238.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 11 | NM_001326299.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 11 | NP_001313228.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 11 | NM_001326299.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 11 | NP_001313228.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 12 | NM_001326300.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 12 | NP_001313229.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 12 | NM_001326300.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 12 | NP_001313229.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 15 | NM_001326303.2:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 15 | NP_001313232.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 15 | NM_001326303.2:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 15 | NP_001313232.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 13 | NM_001326301.2:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 13 | NP_001313230.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 13 | NM_001326301.2:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 13 | NP_001313230.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 16 | NM_001326304.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 16 | NP_001313233.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 16 | NM_001326304.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 16 | NP_001313233.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 23 | NM_001326311.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 23 | NP_001313240.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 23 | NM_001326311.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 23 | NP_001313240.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 25 | NM_001326313.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 25 | NP_001313242.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 25 | NM_001326313.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 25 | NP_001313242.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 22 | NM_001326310.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 22 | NP_001313239.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 22 | NM_001326310.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 22 | NP_001313239.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 6 | NM_001160104.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 6 | NP_001153576.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 6 | NM_001160104.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 6 | NP_001153576.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 19 | NM_001326307.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 19 | NP_001313236.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 19 | NM_001326307.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 19 | NP_001313236.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 2 | NM_207660.4:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 2 | NP_997543.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 2 | NM_207660.4:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 2 | NP_997543.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 9 | NM_001326297.2:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 9 | NP_001313226.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 9 | NM_001326297.2:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 9 | NP_001313226.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 7 | NM_001326295.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 7 | NP_001313224.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 7 | NM_001326295.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 7 | NP_001313224.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 10 | NM_001326298.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 10 | NP_001313227.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 10 | NM_001326298.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 10 | NP_001313227.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 24 | NM_001326312.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 24 | NP_001313241.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 24 | NM_001326312.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 24 | NP_001313241.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 27 | NM_001326315.2:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313244.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 27 | NM_001326315.2:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313244.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 5 | NM_001160103.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 5 | NP_001153575.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 5 | NM_001160103.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 5 | NP_001153575.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 26 | NM_001326314.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 26 | NP_001313243.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 26 | NM_001326314.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 26 | NP_001313243.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 18 | NM_001326306.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 18 | NP_001313235.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 18 | NM_001326306.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 18 | NP_001313235.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 17 | NM_001326305.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 17 | NP_001313234.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 17 | NM_001326305.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 17 | NP_001313234.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 14 | NM_001326302.2:c.491A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 14 | NP_001313231.1:p.Asp164Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 14 | NM_001326302.2:c.491A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 14 | NP_001313231.1:p.Asp164Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 8 | NM_001326296.2:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 8 | NP_001313225.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 8 | NM_001326296.2:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 8 | NP_001313225.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 28 | NM_001326316.2:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313245.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 28 | NM_001326316.2:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313245.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 3 | NM_207661.3:c.854A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 3 | NP_997544.1:p.Asp285Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant 3 | NM_207661.3:c.854A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform 3 | NP_997544.1:p.Asp285Gly | D (Asp) > G (Gly) | Missense Variant |
| ZC3H14 transcript variant 29 | NR_136936.2:n.1053A>C | N/A | Non Coding Transcript Variant |
| ZC3H14 transcript variant 29 | NR_136936.2:n.1053A>G | N/A | Non Coding Transcript Variant |
| ZC3H14 transcript variant X1 | XM_011537162.4:c.956A>C | D [GAT] > A [GCT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform X1 | XP_011535464.1:p.Asp319Ala | D (Asp) > A (Ala) | Missense Variant |
| ZC3H14 transcript variant X1 | XM_011537162.4:c.956A>G | D [GAT] > G [GGT] | Coding Sequence Variant |
| zinc finger CCCH domain-containing protein 14 isoform X1 | XP_011535464.1:p.Asp319Gly | D (Asp) > G (Gly) | Missense Variant |
Help
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Not Reported in ClinVar
Help
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | A= | C | G |
|---|---|---|---|
| GRCh38.p14 chr 14 | NC_000014.9:g.88574787= | NC_000014.9:g.88574787A>C | NC_000014.9:g.88574787A>G |
| GRCh37.p13 chr 14 | NC_000014.8:g.89041131= | NC_000014.8:g.89041131A>C | NC_000014.8:g.89041131A>G |
| ZC3H14 RefSeqGene | NG_050601.1:g.16879= | NG_050601.1:g.16879A>C | NG_050601.1:g.16879A>G |
| ZC3H14 transcript variant 1 | NM_024824.4:c.956= | NM_024824.4:c.956A>C | NM_024824.4:c.956A>G |
| ZC3H14 transcript variant 1 | NM_024824.5:c.956= | NM_024824.5:c.956A>C | NM_024824.5:c.956A>G |
| ZC3H14 transcript variant 3 | NM_207661.2:c.854= | NM_207661.2:c.854A>C | NM_207661.2:c.854A>G |
| ZC3H14 transcript variant 3 | NM_207661.3:c.854= | NM_207661.3:c.854A>C | NM_207661.3:c.854A>G |
| ZC3H14 transcript variant 28 | NM_001326316.1:c.854= | NM_001326316.1:c.854A>C | NM_001326316.1:c.854A>G |
| ZC3H14 transcript variant 28 | NM_001326316.2:c.854= | NM_001326316.2:c.854A>C | NM_001326316.2:c.854A>G |
| ZC3H14 transcript variant 2 | NM_207660.4:c.956= | NM_207660.4:c.956A>C | NM_207660.4:c.956A>G |
| ZC3H14 transcript variant 2 | NM_207660.3:c.956= | NM_207660.3:c.956A>C | NM_207660.3:c.956A>G |
| ZC3H14 transcript variant X1 | XM_011537162.4:c.956= | XM_011537162.4:c.956A>C | XM_011537162.4:c.956A>G |
| ZC3H14 transcript variant X3 | XM_011537162.3:c.956= | XM_011537162.3:c.956A>C | XM_011537162.3:c.956A>G |
| ZC3H14 transcript variant X11 | XM_011537162.2:c.956= | XM_011537162.2:c.956A>C | XM_011537162.2:c.956A>G |
| ZC3H14 transcript variant X8 | XM_011537162.1:c.956= | XM_011537162.1:c.956A>C | XM_011537162.1:c.956A>G |
| ZC3H14 transcript variant 9 | NM_001326297.2:c.854= | NM_001326297.2:c.854A>C | NM_001326297.2:c.854A>G |
| ZC3H14 transcript variant 9 | NM_001326297.1:c.854= | NM_001326297.1:c.854A>C | NM_001326297.1:c.854A>G |
| ZC3H14 transcript variant 27 | NM_001326315.2:c.854= | NM_001326315.2:c.854A>C | NM_001326315.2:c.854A>G |
| ZC3H14 transcript variant 27 | NM_001326315.1:c.854= | NM_001326315.1:c.854A>C | NM_001326315.1:c.854A>G |
| ZC3H14 transcript variant 13 | NM_001326301.2:c.854= | NM_001326301.2:c.854A>C | NM_001326301.2:c.854A>G |
| ZC3H14 transcript variant 13 | NM_001326301.1:c.854= | NM_001326301.1:c.854A>C | NM_001326301.1:c.854A>G |
| ZC3H14 transcript variant 5 | NM_001160103.2:c.956= | NM_001160103.2:c.956A>C | NM_001160103.2:c.956A>G |
| ZC3H14 transcript variant 5 | NM_001160103.1:c.956= | NM_001160103.1:c.956A>C | NM_001160103.1:c.956A>G |
| ZC3H14 transcript variant 22 | NM_001326310.2:c.956= | NM_001326310.2:c.956A>C | NM_001326310.2:c.956A>G |
| ZC3H14 transcript variant 22 | NM_001326310.1:c.956= | NM_001326310.1:c.956A>C | NM_001326310.1:c.956A>G |
| ZC3H14 transcript variant 6 | NM_001160104.2:c.956= | NM_001160104.2:c.956A>C | NM_001160104.2:c.956A>G |
| ZC3H14 transcript variant 6 | NM_001160104.1:c.956= | NM_001160104.1:c.956A>C | NM_001160104.1:c.956A>G |
| ZC3H14 transcript variant 19 | NM_001326307.2:c.956= | NM_001326307.2:c.956A>C | NM_001326307.2:c.956A>G |
| ZC3H14 transcript variant 19 | NM_001326307.1:c.956= | NM_001326307.1:c.956A>C | NM_001326307.1:c.956A>G |
| ZC3H14 transcript variant 8 | NM_001326296.2:c.956= | NM_001326296.2:c.956A>C | NM_001326296.2:c.956A>G |
| ZC3H14 transcript variant 8 | NM_001326296.1:c.956= | NM_001326296.1:c.956A>C | NM_001326296.1:c.956A>G |
| ZC3H14 transcript variant 24 | NM_001326312.2:c.956= | NM_001326312.2:c.956A>C | NM_001326312.2:c.956A>G |
| ZC3H14 transcript variant 24 | NM_001326312.1:c.956= | NM_001326312.1:c.956A>C | NM_001326312.1:c.956A>G |
| ZC3H14 transcript variant 11 | NM_001326299.2:c.956= | NM_001326299.2:c.956A>C | NM_001326299.2:c.956A>G |
| ZC3H14 transcript variant 11 | NM_001326299.1:c.956= | NM_001326299.1:c.956A>C | NM_001326299.1:c.956A>G |
| ZC3H14 transcript variant 12 | NM_001326300.2:c.491= | NM_001326300.2:c.491A>C | NM_001326300.2:c.491A>G |
| ZC3H14 transcript variant 12 | NM_001326300.1:c.491= | NM_001326300.1:c.491A>C | NM_001326300.1:c.491A>G |
| ZC3H14 transcript variant 14 | NM_001326302.2:c.491= | NM_001326302.2:c.491A>C | NM_001326302.2:c.491A>G |
| ZC3H14 transcript variant 14 | NM_001326302.1:c.491= | NM_001326302.1:c.491A>C | NM_001326302.1:c.491A>G |
| ZC3H14 transcript variant 29 | NR_136936.2:n.1053= | NR_136936.2:n.1053A>C | NR_136936.2:n.1053A>G |
| ZC3H14 transcript variant 29 | NR_136936.1:n.1181= | NR_136936.1:n.1181A>C | NR_136936.1:n.1181A>G |
| ZC3H14 transcript variant 17 | NM_001326305.2:c.491= | NM_001326305.2:c.491A>C | NM_001326305.2:c.491A>G |
| ZC3H14 transcript variant 17 | NM_001326305.1:c.491= | NM_001326305.1:c.491A>C | NM_001326305.1:c.491A>G |
| ZC3H14 transcript variant 26 | NM_001326314.2:c.491= | NM_001326314.2:c.491A>C | NM_001326314.2:c.491A>G |
| ZC3H14 transcript variant 26 | NM_001326314.1:c.491= | NM_001326314.1:c.491A>C | NM_001326314.1:c.491A>G |
| ZC3H14 transcript variant 15 | NM_001326303.2:c.854= | NM_001326303.2:c.854A>C | NM_001326303.2:c.854A>G |
| ZC3H14 transcript variant 15 | NM_001326303.1:c.854= | NM_001326303.1:c.854A>C | NM_001326303.1:c.854A>G |
| ZC3H14 transcript variant 7 | NM_001326295.2:c.956= | NM_001326295.2:c.956A>C | NM_001326295.2:c.956A>G |
| ZC3H14 transcript variant 7 | NM_001326295.1:c.956= | NM_001326295.1:c.956A>C | NM_001326295.1:c.956A>G |
| ZC3H14 transcript variant 10 | NM_001326298.2:c.956= | NM_001326298.2:c.956A>C | NM_001326298.2:c.956A>G |
| ZC3H14 transcript variant 10 | NM_001326298.1:c.956= | NM_001326298.1:c.956A>C | NM_001326298.1:c.956A>G |
| ZC3H14 transcript variant 20 | NM_001326308.2:c.491= | NM_001326308.2:c.491A>C | NM_001326308.2:c.491A>G |
| ZC3H14 transcript variant 20 | NM_001326308.1:c.491= | NM_001326308.1:c.491A>C | NM_001326308.1:c.491A>G |
| ZC3H14 transcript variant 16 | NM_001326304.2:c.491= | NM_001326304.2:c.491A>C | NM_001326304.2:c.491A>G |
| ZC3H14 transcript variant 16 | NM_001326304.1:c.491= | NM_001326304.1:c.491A>C | NM_001326304.1:c.491A>G |
| ZC3H14 transcript variant 21 | NM_001326309.2:c.491= | NM_001326309.2:c.491A>C | NM_001326309.2:c.491A>G |
| ZC3H14 transcript variant 21 | NM_001326309.1:c.491= | NM_001326309.1:c.491A>C | NM_001326309.1:c.491A>G |
| ZC3H14 transcript variant 23 | NM_001326311.2:c.491= | NM_001326311.2:c.491A>C | NM_001326311.2:c.491A>G |
| ZC3H14 transcript variant 23 | NM_001326311.1:c.491= | NM_001326311.1:c.491A>C | NM_001326311.1:c.491A>G |
| ZC3H14 transcript variant 25 | NM_001326313.2:c.956= | NM_001326313.2:c.956A>C | NM_001326313.2:c.956A>G |
| ZC3H14 transcript variant 25 | NM_001326313.1:c.956= | NM_001326313.1:c.956A>C | NM_001326313.1:c.956A>G |
| ZC3H14 transcript variant 18 | NM_001326306.2:c.956= | NM_001326306.2:c.956A>C | NM_001326306.2:c.956A>G |
| ZC3H14 transcript variant 18 | NM_001326306.1:c.956= | NM_001326306.1:c.956A>C | NM_001326306.1:c.956A>G |
| zinc finger CCCH domain-containing protein 14 isoform 1 | NP_079100.2:p.Asp319= | NP_079100.2:p.Asp319Ala | NP_079100.2:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 3 | NP_997544.1:p.Asp285= | NP_997544.1:p.Asp285Ala | NP_997544.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313245.1:p.Asp285= | NP_001313245.1:p.Asp285Ala | NP_001313245.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 2 | NP_997543.1:p.Asp319= | NP_997543.1:p.Asp319Ala | NP_997543.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform X1 | XP_011535464.1:p.Asp319= | XP_011535464.1:p.Asp319Ala | XP_011535464.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 9 | NP_001313226.1:p.Asp285= | NP_001313226.1:p.Asp285Ala | NP_001313226.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 27 | NP_001313244.1:p.Asp285= | NP_001313244.1:p.Asp285Ala | NP_001313244.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 13 | NP_001313230.1:p.Asp285= | NP_001313230.1:p.Asp285Ala | NP_001313230.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 5 | NP_001153575.1:p.Asp319= | NP_001153575.1:p.Asp319Ala | NP_001153575.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 22 | NP_001313239.1:p.Asp319= | NP_001313239.1:p.Asp319Ala | NP_001313239.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 6 | NP_001153576.1:p.Asp319= | NP_001153576.1:p.Asp319Ala | NP_001153576.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 19 | NP_001313236.1:p.Asp319= | NP_001313236.1:p.Asp319Ala | NP_001313236.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 8 | NP_001313225.1:p.Asp319= | NP_001313225.1:p.Asp319Ala | NP_001313225.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 24 | NP_001313241.1:p.Asp319= | NP_001313241.1:p.Asp319Ala | NP_001313241.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 11 | NP_001313228.1:p.Asp319= | NP_001313228.1:p.Asp319Ala | NP_001313228.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 12 | NP_001313229.1:p.Asp164= | NP_001313229.1:p.Asp164Ala | NP_001313229.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 14 | NP_001313231.1:p.Asp164= | NP_001313231.1:p.Asp164Ala | NP_001313231.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 17 | NP_001313234.1:p.Asp164= | NP_001313234.1:p.Asp164Ala | NP_001313234.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 26 | NP_001313243.1:p.Asp164= | NP_001313243.1:p.Asp164Ala | NP_001313243.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 15 | NP_001313232.1:p.Asp285= | NP_001313232.1:p.Asp285Ala | NP_001313232.1:p.Asp285Gly |
| zinc finger CCCH domain-containing protein 14 isoform 7 | NP_001313224.1:p.Asp319= | NP_001313224.1:p.Asp319Ala | NP_001313224.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 10 | NP_001313227.1:p.Asp319= | NP_001313227.1:p.Asp319Ala | NP_001313227.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 20 | NP_001313237.1:p.Asp164= | NP_001313237.1:p.Asp164Ala | NP_001313237.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 16 | NP_001313233.1:p.Asp164= | NP_001313233.1:p.Asp164Ala | NP_001313233.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 21 | NP_001313238.1:p.Asp164= | NP_001313238.1:p.Asp164Ala | NP_001313238.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 23 | NP_001313240.1:p.Asp164= | NP_001313240.1:p.Asp164Ala | NP_001313240.1:p.Asp164Gly |
| zinc finger CCCH domain-containing protein 14 isoform 25 | NP_001313242.1:p.Asp319= | NP_001313242.1:p.Asp319Ala | NP_001313242.1:p.Asp319Gly |
| zinc finger CCCH domain-containing protein 14 isoform 18 | NP_001313235.1:p.Asp319= | NP_001313235.1:p.Asp319Ala | NP_001313235.1:p.Asp319Gly |
Help
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
1 SubSNP,
2 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2740878974 | Nov 08, 2017 (151) |
| 2 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 3 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
Help
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Help
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1487293579
Help
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genome context:
Select flank length:
Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.